DWZ
- Product code
- DWZ
- Device name
- Device, Biopsy, Endomyocardial
- Device class
- Class 2
- 21 CFR
- 21 CFR 870.4075
- Medical specialty
- Cardiovascular
- Marketing pathway
- 510(K)
- Flag
- Third-party review eligible
- 510(k) clearances (last 3 years)
- 23
510(k) clearances, last 3 years (1)
| Number | Decision date | Applicant | Device name | Summary |
|---|---|---|---|---|
| K252722 | 2025-09-30 | Fehling Instruments GmbH | Biopsy Forceps |
Official FDA classification page: DWZ
Classification and pathway per current FDA publications. Data from openFDA (CC0).